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Non-deletional alpha thalassaemia: a review

Orphanet journal of rare diseases, 2020-06, Vol.15 (1), p.166-12, Article 166

2020

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Potential Point-of-Care Microfluidic Devices to Diagnose Iron Deficiency Anemia

Sensors (Basel, Switzerland), 2018-08, Vol.18 (8), p.2625

2018

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Defects in nerve conduction velocity and different muscle fibre-type specificity contribute to muscle weakness in Ts1Cje Down syndrome mouse model

PloS one, 2018-05, Vol.13 (5), p.e0197711-e0197711

2018

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Functional transcriptome analysis of the postnatal brain of the Ts1Cje mouse model for Down syndrome reveals global disruption of interferon-related molecular networks

BMC genomics, 2014-07, Vol.15 (1), p.624-624

2014

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Molecular basis of transfusion dependent beta-thalassemia major patients in Sabah

Journal of human genetics, 2014-03, Vol.59 (3), p.119-123

2014

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cMYB is involved in the regulation of fetal hemoglobin production in adults

Blood, 2006-08, Vol.108 (3), p.1077-1083

2006

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Haplotype Analysis of β-Thalassaemia Major and Carriers with Filipino β°-Deletion in Sabah, Malaysia

The Malaysian journal of medical sciences, 2018-07, Vol.25 (4), p.63-71

2018

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Molecular pathways governing development of vascular endothelial cells from ES/iPS cells

Stem cell reviews, 2013-10, Vol.9 (5), p.586-598

2013

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EVALUATION OF RED BLOOD CELL INDICES RELATED DISORDERS AMONG ELIGIBLE BLOOD DONORS AT THE UNIVERSITI PUTRA MALAYSIA (UPM)

Southeast Asian journal of tropical medicine and public health, 2015-09, Vol.46 (5), p.911-917

2015

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Localized SCF and IGF-1 secretion enhances erythropoiesis in the spleen of murine embryos

Biology open, 2015-05, Vol.4 (5), p.596-607

2015

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Correlation of BACH1 and Hemoglobin E/Beta-Thalassemia Globin Expression

Turkish journal of haematology, 2016-03, Vol.33 (1), p.15-20

2016

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The Novel Role of the B-Cell Lymphoma/Leukemia 11A (BCL11A) Gene in β-Thalassaemia Treatment

Cardiovascular & hematological disorders drug targets, 2022-12, Vol.22 (4), p.226-236

2022

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Hematopoietic cell differentiation from embryonic and induced pluripotent stem cells

Stem cell research & therapy, 2013-06, Vol.4 (3), p.71-71, Article 71

2013

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Artificial Intelligence in Pathology

Malaysian Journal of Medicine and Health Sciences, 2023-12, Vol.19 (s16), p.1-2

2023

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A Twins Heritability Study on Alpha Hemoglobin Stabilizing Protein (AHSP) Expression Variability

Twin research and human genetics, 2010-12, Vol.13 (6), p.567-572

2010

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Transgene expression from CpG-reduced lentiviral gene delivery vectors in vitro

Gene, 2014-01, Vol.533 (1), p.451-455

2014

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HbF in HbE/β-thalassemia: A clinical and laboratory correlation

Hematology (Luxembourg), 2015-07, Vol.20 (6), p.349-353

2015

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Advancements in reprogramming strategies for the generation of induced pluripotent stem cells

Journal of assisted reproduction and genetics, 2011-04, Vol.28 (4), p.291-301

2011

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Iron deficiency anaemia: with the conclusion of a need for iron reader

Journal of physics. Conference series, 2017-10, Vol.914 (1), p.12028

2017

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α‐Haemoglobin stabilising protein is a quantitative trait gene that modifies the phenotype of β‐thalassaemia

British journal of haematology, 2006-06, Vol.133 (6), p.675-682

2006

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α-Haemoglobin stabilising protein expression is influenced by mean cell haemoglobin and HbF levels in HbE/β-thalassaemia individuals

Blood cells, molecules, & diseases, 2012-01, Vol.48 (1), p.17-21

2012

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HbA2 levels in β-thalassaemia carriers with the Filipino β0-deletion: are the levels higher than what is found with non-deletional forms of β0-thalassaemia?

Pathology, 2013-01, Vol.45 (1), p.62-65

2013

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Data-based Decision Making in Education: Challenges and Opportunities

Springer, 2012, Vol.17

1. Aufl., 2012

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Bach1 : A possible player in HbE/beta thalassaemia?

Asian Pacific journal of tropical disease, 2014-06, Vol.4 (3), p.239-239

2014

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Lack of methylation on transgene leads to high level and persistent transgene expression in induced pluripotent stem cells

Gene, 2020-10, Vol.758, p.144958-144958, Article 144958

2020

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Non-deletional alpha thalassaemia: a review

Potential Point-of-Care Microfluidic Devices to Diagnose Iron Deficiency Anemia

Defects in nerve conduction velocity and different muscle fibre-type specificity contribute to muscle weakness in Ts1Cje Down syndrome mouse model

Functional transcriptome analysis of the postnatal brain of the Ts1Cje mouse model for Down syndrome reveals global disruption of interferon-related molecular networks

Molecular basis of transfusion dependent beta-thalassemia major patients in Sabah

cMYB is involved in the regulation of fetal hemoglobin production in adults

Haplotype Analysis of β-Thalassaemia Major and Carriers with Filipino β°-Deletion in Sabah, Malaysia

Molecular pathways governing development of vascular endothelial cells from ES/iPS cells

EVALUATION OF RED BLOOD CELL INDICES RELATED DISORDERS AMONG ELIGIBLE BLOOD DONORS AT THE UNIVERSITI PUTRA MALAYSIA (UPM)

Localized SCF and IGF-1 secretion enhances erythropoiesis in the spleen of murine embryos

Correlation of BACH1 and Hemoglobin E/Beta-Thalassemia Globin Expression

The Novel Role of the B-Cell Lymphoma/Leukemia 11A (BCL11A) Gene in β-Thalassaemia Treatment

Hematopoietic cell differentiation from embryonic and induced pluripotent stem cells

Artificial Intelligence in Pathology

A Twins Heritability Study on Alpha Hemoglobin Stabilizing Protein (AHSP) Expression Variability

Transgene expression from CpG-reduced lentiviral gene delivery vectors in vitro

HbF in HbE/β-thalassemia: A clinical and laboratory correlation

Advancements in reprogramming strategies for the generation of induced pluripotent stem cells

Iron deficiency anaemia: with the conclusion of a need for iron reader

α‐Haemoglobin stabilising protein is a quantitative trait gene that modifies the phenotype of β‐thalassaemia

α-Haemoglobin stabilising protein expression is influenced by mean cell haemoglobin and HbF levels in HbE/β-thalassaemia individuals

HbA2 levels in β-thalassaemia carriers with the Filipino β0-deletion: are the levels higher than what is found with non-deletional forms of β0-thalassaemia?

Data-based Decision Making in Education: Challenges and Opportunities

Bach1 : A possible player in HbE/beta thalassaemia?

Lack of methylation on transgene leads to high level and persistent transgene expression in induced pluripotent stem cells

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